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  Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist.

Rettinger, J., Braun, K., Hochmann, H., Kassack, M. U., Ullmann, H., Nickel, P., et al. (2005). Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist. Neuropharmacology, 48(3), 461-468.

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 Creators:
Rettinger, Jürgen1, Author           
Braun, Kirsten, Author
Hochmann, Henrike, Author
Kassack, Matthias U., Author
Ullmann, Heiko, Author
Nickel, Peter, Author
Schmalzing, Günther, Author
Lambrecht, Günter, Author
Affiliations:
1Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society, ou_2068289              

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Language(s): eng - English
 Dates: 2005-03
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 263000
 Degree: -

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Title: Neuropharmacology
Source Genre: Journal
 Creator(s):
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Pages: - Volume / Issue: 48 (3) Sequence Number: - Start / End Page: 461 - 468 Identifier: -